CIP29 Antibody
CATALOG NUMBER: 30-653- Clonality: Polyclonal
- Tested Applications: ELISA, WB
- Host Species: Rabbit
- Species Reactivity: Human, Mouse, Rat
- Conjugate: Unconjugated
- Size: 100 ul
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- HOST SPECIES: Rabbit
- SPECIES REACTIVITY: Human, Mouse, Rat
- IMMUNOGEN: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human CIP29.
- CONJUGATE: Unconjugated
- TESTED APPLICATIONS: ELISA, WB
- APPLICATION NOTE: CIP29 antibody can be used for detection of CIP29 by ELISA at 1:1562500. CIP29 antibody can be used for detection of CIP29 by western blot at 0.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- POSITIVE CONTROL 1: Cat. No. 1211 - HepG2 Cell Lysate
- PREDICTED MOLECULAR WEIGHT: 24 kDa
Properties
- PURIFICATION: Antibody is purified by peptide affinity chromatography method.
- CLONALITY: Polyclonal
- PHYSICAL STATE: Liquid
- BUFFER: Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
- CONCENTRATION: batch dependent
- STORAGE CONDITIONS: For short periods of storage (days) store at 4°C. For longer periods of storage, store CIP29 antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Additional Info
- NCBI OFFICIAL SYMBOL: SARNP
- ADDITIONAL NAMES: CIP29, HCC-1, HCC1, HSPC316, MGC14726, THO1, CIP29
- Protein Accession Number: NP_149073
- PROTEIN GI NUMBER: 32129199
- NCBI GENE ID NUMBER: 84324
- USER NOTE: Optimal dilutions for each application to be determined by the researcher.
Background
- CIP29 physically and functionally associates with DDX39, suggesting their cooperation in the RNA metabolism. CIP29 appears to be a new cytokine regulated protein involved in normal and cancer cell proliferation.
- 1: Sugiura, T., (2007) Exp. Cell Res. 313 (4), 782-790.
Disclaimer
- FOR RESEARCH USE ONLY
For additional information, visit ProSci's Terms & Conditions Page. - Disclaimer: This product is for research use only.
Shipping Info
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$35 Dry Ice Shipment fee may be required on some items.
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